Elucidation of the timescales and origins of quantum electronic coherence in LHCII
Nature chemistry, 2012•nature.com
Photosynthetic organisms harvest sunlight with near unity quantum efficiency. The
complexity of the electronic structure and energy transfer pathways within networks of
photosynthetic pigment–protein complexes often obscures the mechanisms behind the
efficient light-absorption-to-charge conversion process. Recent experiments, particularly
using two-dimensional spectroscopy, have detected long-lived quantum coherence, which
theory suggests may contribute to the effectiveness of photosynthetic energy transfer. Here …
complexity of the electronic structure and energy transfer pathways within networks of
photosynthetic pigment–protein complexes often obscures the mechanisms behind the
efficient light-absorption-to-charge conversion process. Recent experiments, particularly
using two-dimensional spectroscopy, have detected long-lived quantum coherence, which
theory suggests may contribute to the effectiveness of photosynthetic energy transfer. Here …
Abstract
Photosynthetic organisms harvest sunlight with near unity quantum efficiency. The complexity of the electronic structure and energy transfer pathways within networks of photosynthetic pigment–protein complexes often obscures the mechanisms behind the efficient light-absorption-to-charge conversion process. Recent experiments, particularly using two-dimensional spectroscopy, have detected long-lived quantum coherence, which theory suggests may contribute to the effectiveness of photosynthetic energy transfer. Here, we present a new, direct method to access coherence signals: a coherence-specific polarization sequence, which isolates the excitonic coherence features from the population signals that usually dominate two-dimensional spectra. With this polarization sequence, we elucidate coherent dynamics and determine the overall measurable lifetime of excitonic coherence in the major light-harvesting complex of photosystem II. Coherence decays on two distinct timescales of 47 fs and ~800 fs. We present theoretical calculations to show that these two timescales are from weakly and moderately strongly coupled pigments, respectively.
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